Canonical Allele Identifier: PA2580545570
Gene: CCDC39 HGNC NCBI

Linked Data

ClinVar Variation Id: 2397672
ClinVar RCV Id: RCV004233382

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_852091.1:p.Arg214Gly
CA2716116
NM_181426.2:c.640C>G